Title Revenue Accountant Employment Type Fixed Term Contract (Dublin/Cork/Hybrid) Key Responsibilities Month and quarter-end close activities, including GTN accrual preparation, balance sheet reconciliations and financial reporting. Validate and process rebate claims in accordance with commercial contracts and accruals. Assist with review and analysis of Commercial Contracts under ASC 606 to ensure appropriate revenue recognition treatment. Support revenue reporting to the Business and collaborate with Legal, Market Access, Commercial Operations and Finance for ex‑US commercial and payer contract structure to assess revenue recognition impact under ASC 606. Support the year‑end financial audit and the SOX audit. Assist with preparation of SEC Reports for 10Q filing. Assist with ad hoc financial analysis, queries and activities as required. Work closely with Finance colleagues both locally and globally, adhering to global deadlines. Experience Proven experience in revenue accounting or a similar finance role. Proficiency in accounting software and MS Office Suite, particularly Excel. Excellent attention to detail and analytical skills. Ability to meet deadlines and work effectively under pressure. Strong communication and collaboration skills. Familiarity with Sarbanes‑Oxley and internal controls is desirable. Experience with SAP S4 Hana / Vistex is advantageous. Results orientated, flexible, resourceful, & self‑motivated with the ability to manage multiple deliverables. Education Degree in Accounting, Finance, or related field. Fully Qualified Accountant (ACA or ACCA preferred) Seniority level Associate Job function Accounting/Auditing and Finance Industries Financial Services and Accounting Join our team Join our team and contribute to accurate revenue management that supports our company’s growth and success! #J-18808-Ljbffr
A leading pharmaceutical company based in Cork is seeking a Maintenance Technician. This role involves maintaining process, utility, and facility equipment in accordance with cGMP regulations, managing vendor support, and performing root cause analysis. The ideal candidate has a relevant engineering qualification and at least 3 years of experience in a GMP environment. This position offers a contract role within the pharmaceutical manufacturing industry. #J-18808-Ljbffr
Proactively maintain process, utility and facility equipment in accordance with cGMP regulations, applicable safety considerations, Standard Operating Procedures, best maintenance practices and the reliability agenda. Maintenance and troubleshooting of equipment. Interact with all process partners to continuously improve operations by recognising and correcting the causes of less than optimal equipment, facility and team performance. Manage external vendor support to complete required services in a GMP compliant manner. Perform problem solving including root cause analysis as required when equipment failures result in loss of production, substandard equipment performance and substantial repair cost and/or personnel safety incidents. Ensure Electrical, Process and Utility Systems are maintained in a controlled state thus ensuring compliance with all procedures and regulations and reliability initiatives. Maintain a safe working environment by continuously promoting safety awareness, recognising and rectifying unsafe conditions and performing thorough investigations when accidents occur. Record all maintenance work performed on the site CMMS system. Respond to critical utility alarms generated from the site automated alarm messenger system. Maintain documentation and management and control systems in compliance with cGMP regulations and training instructions. Where required complete and record calibrations activities completed on site and report any defects detected. Contribute to the drive to effectively manage spares, consumables and contracts in a timely and cost effective manner. Use of permit to work system or other safety systems to control engineering activities. Participation in HAZOP and design reviews. SCOPE This position ensures the Manufacturing, Quality Control, and Facilities equipment and instrumentation is maintained & operated in the calibrated state necessary to perform cGMP activities. Maintenance Technician has scope to initiate process, cost and execute continuous improvement ideas. EDUCATION AND EXPERIENCE A relevant third level qualification in Engineering or time-served apprenticeship with 3+ years’ experience in a GMP environment, preferably Bio-pharmaceuticals or equivalent industry with drug product fill finishing and packaging activities. Seniority Level Associate Employment Type Contract Job Function Health Care Provider Industry Pharmaceutical Manufacturing #J-18808-Ljbffr
Our Biopharmaceutical client is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life‑threatening rare genetic diseases. They target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. Onsite role - 2 Shift 12 Month Contract ROLE Reporting to the Packaging Team Lead, the Packaging Technician is responsible for the day‑to‑day operation of the packaging suite. The Packaging Technician will work in a team environment with an emphasis on safety and quality, and with a commitment to continuous improvement. KEY RESPONSIBILITIES Work as part of a team of Packaging Technicians to complete the packaging of finished Produce for onward distribution. Detailed batch record keeping which is accurate, complete, legible and in accordance with cGMP requirements. Identify issues on the line and alert the Packaging Equipment Technician. Provide support to the Packaging Equipment Technician to help resolve issues on the line as required. Carry out transactions on SAP as required. Ensure the Packaging area is Inspection Ready at all times. Participate in Regulatory Inspections. Assist with writing, reviewing and revision of packing documentation as necessary (e.g. batch records, standard operating procedure etc). Demonstrate commitment to a high level of safety awareness with the Packaging Operations Team. Proactively support continuous improvement and lead initiatives with the Packaging Suite. Lead and support the investigation and resolutions of process investigations. Maintain an exemplary personal training record. Execute all operations activities in a safe manner and in strict accordance with SOPs, cGMP regulations and Site Quality Standards. EDUCATION AND EXPERIENCE Previous experience in a highly regulated operating environment, such as the pharmaceutical or medical device sectors, is desirable though not essential. Previous packaging experience will be considered advantageous. Demonstrated experience (2+ years) of operating in a team environment (professional) is required. Candidates who can demonstrate a keen sense of focus and attention to detail when fulfilling exacting and repetitious tasks will have a distinct advantage. Must be conscientious and possess strong teamwork and interpersonal skills. Strong communication and problem‑solving skills are highly valued. The Packaging Technician will be required to work closely within a cross‑functional team, including other Packaging Technicians, Packaging Equipment Technicians and representation from Quality, Material Operations (warehouse) and others. Note: This description is not intended to be all‑inclusive or a limitation of the duties of the position. It is intended to describe the general nature of the job that may include other duties as assumed or assigned. Job Details Seniority level: Entry level Employment type: Full‑time Job function: Manufacturing Industries: Pharmaceutical Manufacturing and Manufacturing #J-18808-Ljbffr
Tax Manager / Senior Manager Our Biopharmaceutical client is the world leader in delivering therapeutics that provide meaningful advances to patients who live with serious and life‑threatening rare genetic diseases. They target diseases that lack effective therapies and affect relatively small numbers of patients, many of whom are children. These conditions are often inherited, difficult to diagnose, progressively debilitating and have few, if any, treatment options. Location: Cork / Dublin (hybrid) Contract: 12 Month Contract Role Summary The tax team is seeking a highly talented and motivated Tax Manager/Senior Manager to support the direct tax compliance and provisioning process for up to 25 entities in the EMEA region. The ideal candidate will have previous corporate tax experience in a multinational/Big 4 environment and be looking to broaden experience in a dynamic, fast‑paced environment. Responsibilities Manage quarterly and yearly current and deferred tax provisions for group reporting under US GAAP and annual statutory disclosures under IFRS for multiple group companies, including preparation and review of workings and coordination with EMEA and Global Tax and Finance teams, financial auditors, and local advisors. Partner with wider Finance teams on statutory account preparation. Oversee external service providers to meet corporate and withholding tax compliance and payment obligations across jurisdictions, assisted by the Senior Tax Analyst. Manage the R&D tax credit process, preparing calculations, liaising with internal teams and external advisors. Collaborate with Treasury to ensure appropriate funding, hedging for upcoming tax payments, and proposed investment strategies. Develop and maintain strong relationships with internal stakeholders, external tax advisors, and local tax authorities. Work closely with Legal, Finance and broader business to provide commercially focused and actionable tax guidance. Assist EMEA and Global Tax Teams with tax projects such as system implementation/automation and continuous improvement initiatives. Support the Tax Director and Global Tax team on tax planning strategies and opportunities. Stay current with legislative developments and ensure implications are addressed appropriately. Support and manage tax audits/enquiries as they arise. Perform additional tax department tasks including process documentation, compliance and risk tracking, and supplier engagement and fee management. Other duties as assigned. Education Required Ireland Tax Institute qualified / Qualified accountant (ACA, ACCA or CIMA) Undergraduate Degree in Business, Finance, or Accounting Experience Required Minimum 6 years corporate tax experience, preferably in a multinational environment. Proficient in Microsoft Office, especially Outlook, Excel, Word, and Power BI. ERP experience, ideally Oracle or SAP. Experience with data analytics tools or tax software is an advantage. Strong attention to detail, analytical skills, initiative, and ability to adhere to strict timelines. Ability to work well in a team, influence cross‑functional groups, and develop effective working relationships. Experience in managing and mentoring. Ability to embrace change and be flexible to changing business needs. Self‑motivated and results‑oriented strategic thinker with solid business understanding. Strong interpersonal, written, and oral communication skills. Seniority level Mid‑Senior level Employment type Full‑time Job function Accounting / Auditing Industries: Accounting and Financial Services #J-18808-Ljbffr
Reporting to management, this Clinical Research Specialist will contribute to one or more clinical studies within the Clinical R&D team, collaborating closely with colleagues throughout the organization. Key Duties & Responsibilities Provide operational support for company-sponsored clinical studies, helping ensure adherence to project deadlines and established milestones, under guidance. Assist in evaluating, launching, managing, and closing clinical trials within designated regions, complying with ICH-GCP guidelines, local legislation, and organizational Standard Operating Procedures. Potentially act as the main point of contact for research sites, including site management activities. Support the development and maintenance of essential clinical trial documentation—including protocols, informed consent forms, case report forms, monitoring plans, study manuals, investigator brochures, and annual progress reports. Facilitate trial registration and post-study reporting (e.g., on clinicaltrials.gov) and aid publication efforts as required. Handle ordering, tracking, and oversight of investigational devices and other study materials. Engage and collaborate with site staff, ethical review boards, external partners/vendors, and internal personnel. Work closely with Clinical Research Associates (CRAs) and other team members. Assist in preparing and managing investigator agreements and processing payments related to clinical studies. Support the review and preparation of clinical data for statistical analysis and publication purposes. May perform site management visits, including site qualification, initiation, interim monitoring, or closure visits as needed by the study. Provide on-site guidance to ensure protocol compliance and accurate data collection. Help oversee and monitor assigned budget allocations for projects. Serve as a dependable source of accurate, current project information for stakeholders. Build a comprehensive understanding of the development pipeline, product portfolio, and business objectives. Typically operates with supervision; makes independent decisions for routine matters, but seeks advice for complex situations. Relay business-related concerns or opportunities to appropriate management levels. Adhere to all guidelines regarding health, safety, and environmental standards, and ensure compliance by direct reports when applicable. Ensure both personal and organizational compliance with federal, state, local, and internal policies and procedures. Perform additional tasks as assigned. Clinical Safety Coordination (may be included) Coordinate all safety-related aspects of clinical trials. Plan and execute new safety initiatives. Develop safety management plans and workflows for clinical research, within all relevant safety regulations. Collaborate with key stakeholders—such as medical teams, study sites, regulatory affairs, and data management—regarding safety activities in clinical studies. Work with data management teams to ensure prompt notification of safety events. Gather required information regarding safety events with the study team. Team with cross-functional groups (R&D, complaint handling, quality/regulatory affairs, medical affairs, medical safety) to ensure compliance with safety reporting. Facilitate review of clinical safety data alongside study teams and medical counterparts. Manage the study safety communications inbox and coordinate timely reporting of adverse events to regulatory authorities and ethics boards. Prepare safety reports for dissemination to stakeholders, investigators, ethics committees, and regulatory authorities. Aid in the scheduling and organization of safety adjudication processes. Arrange and coordinate safety board meetings, acting as a point of contact for all related queries. Ensure all safety documentation is routed to the appropriate personnel. Education Bachelor’s degree (preferably in Life Sciences, Nursing, Physical Sciences, or Biological Sciences) required. Experience Bachelor’s degree with at least 2 years, or Master’s/PhD with at least 1 year of relevant experience preferred. Previous experience in clinical research or a comparable field desirable. Background in clinical or medical settings advantageous. Experience with medical devices viewed favorably. Seniority Level Associate Employment Type Full-time Job Function Research Industries Medical Equipment Manufacturing #J-18808-Ljbffr
Position Overview The Clinical Study Administrator will play a crucial role in the execution and management of clinical studies for medical device development. This position will ensure the smooth administration of clinical trials through document development, site management, budget oversight, safety coordination, and effective communication with internal and external stakeholders. Key Responsibilities Development of Study Documents Prepare and maintain essential clinical trial documentation, including safety management plans, study protocols, informed consent forms, case report forms (CRFs), monitoring plans, study manuals, investigator brochures, and annual reports. Site Management and Monitoring Oversee clinical trial sites, conduct site monitoring activities, and ensure compliance with study protocols and regulatory requirements. Budget Tracking and On-Site Payments Manage budget-related tasks, track study-related expenditures, and coordinate timely on-site payments. Clinical Data Review Support the collection, verification, and review of clinical data for accuracy, completeness, and readiness for analysis. Trial Registration, IRB Submissions, and Site Contracts Coordinate the registration of trials on applicable platforms, prepare and submit documentation to Institutional Review Boards (IRBs), and assist with site contract negotiations and execution. Clinical Safety Coordination Facilitate clinical trial safety processes through the creation and oversight of safety management plans and ensure proper reporting of safety events. Cross‑Functional Communication Collaborate effectively with global teams across clinical research, regulatory affairs, data management, and other key business functions to support study objectives. Qualifications Bachelor’s degree in life sciences, nursing, public health, or related field (advanced degrees preferred). Prior experience in clinical research administration, preferably in the medical device sector. Proven expertise in developing and managing clinical trial documentation. Hands‑on experience with site management, monitoring practices, IRB submissions, and trial registrations. Skilled in budgeting, payment tracking, and data review. Strong interpersonal and communication skills for collaboration with cross‑functional and global teams. Knowledge of regulatory guidelines (e.g., ICH‑GCP, ISO 14155) and good clinical practice. #J-18808-Ljbffr
